US1770635A - Condensed aromatic sulphonic acids and process of making same - Google Patents

Condensed aromatic sulphonic acids and process of making same Download PDF

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Publication number
US1770635A
US1770635A US268376A US26837628A US1770635A US 1770635 A US1770635 A US 1770635A US 268376 A US268376 A US 268376A US 26837628 A US26837628 A US 26837628A US 1770635 A US1770635 A US 1770635A
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United States
Prior art keywords
sulphonic acids
making same
condensed aromatic
aromatic sulphonic
grams
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US268376A
Inventor
Ian C Somerville
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Rohm and Haas Co
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Rohm and Haas Co
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Priority to US268376A priority Critical patent/US1770635A/en
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C14—SKINS; HIDES; PELTS; LEATHER
    • C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
    • C14C3/00—Tanning; Compositions for tanning
    • C14C3/02—Chemical tanning
    • C14C3/08—Chemical tanning by organic agents
    • C14C3/18—Chemical tanning by organic agents using polycondensation products or precursors thereof
    • C14C3/20—Chemical tanning by organic agents using polycondensation products or precursors thereof sulfonated

Definitions

  • This invention relates to newmatei'ials which have the property of converting raw pelt into leather and which also possess a natural affinity for basic dyestufi's.
  • aromatic hydrocarbons consist ofcondensed sulphonic acids of aromatic hydrocarbons formed by condensing the sulfonated hydrocarbons under mild conditions with furfuraldehyde.
  • aromatic hydrocarbons I include benzene and naphthalene and their alkyl substituted derivatives.
  • Ewample #1 128 grams naphthalene, 128 grams sulfuric acid (100%) are heated together at 130 C. for 6 hoursfwith constant stirring. The mass is cooled and 180 grams of water, added. When the temperature is lowered to 25 C. 48 grams of furfuraldehyde are slowly added over a period of one hour while the temperature is held around 25 C.
  • the reaction mixture is stirred intermittently at 25 C. for a further period of 48 hours.
  • the resulting product may be purified as in Example #2 or may be neutralized with milk of lime and filtered to remove the excess sulfuric acid as the calcium salt.
  • the filtrate contains the calcium salt of the new material.
  • This solution is then acidified with sulfuric acid to liberate the new material, the calcium sulfate formed being filtered ofl".

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Patented July 15, 1930 UNITED STATES PATENT OFFICE IAN C. SOMERVILLE, OF GHELTENHAM, PENNSYLVANIA, ASSIGNOR TO ROHM & HAAS J COMPANY, A CORPORATION OF DELAWARE I CONDENSED AROMATIO SULPHONIO ACIDS AND PROCESS OF MAKING SAME No Drawing.
This invention relates to newmatei'ials which have the property of converting raw pelt into leather and which also possess a natural affinity for basic dyestufi's.
These new compounds consist ofcondensed sulphonic acids of aromatic hydrocarbons formed by condensing the sulfonated hydrocarbons under mild conditions with furfuraldehyde. Under aromatic hydrocarbons I include benzene and naphthalene and their alkyl substituted derivatives.
The invention is illustrated by the following examples but is not confined to these examples.
Ewample #1 128 grams naphthalene, 128 grams sulfuric acid (100%) are heated together at 130 C. for 6 hoursfwith constant stirring. The mass is cooled and 180 grams of water, added. When the temperature is lowered to 25 C. 48 grams of furfuraldehyde are slowly added over a period of one hour while the temperature is held around 25 C.
The reaction mixture is stirred intermittently at 25 C. for a further period of 48 hours.
The resulting product may be purified as in Example #2 or may be neutralized with milk of lime and filtered to remove the excess sulfuric acid as the calcium salt. The filtrate contains the calcium salt of the new material. This solution is then acidified with sulfuric acid to liberate the new material, the calcium sulfate formed being filtered ofl".
\ Ewample #2 128 grams naphthalene, 150 gramssulfuric Application filed April 7, 1928. Serial No. 268,376.
for sulfonation of the naphthalene is also.
possible.
Having now illustrated how my invention is carried into effect I claim 1. As new compounds the furfuraldehyde condensation compounds of the sulphonic acids of aromatic hydrocarbons. 4
2. As new compounds the furfuraldehyde condensation compounds of the sulphonic acids of naphthalene.
3. The process of making furfuraldehyde compounds of sulphonic acids of aromatic hydrocarbons bysulfonating the hydrocarbon and condensing, under mild conditions in presence of sulfuric acid, with furfuraldehyde.
4. As .new compounds the furfuraldehyde condensation compounds of the sulphonic acids of a member of the group consisting of naphthalene and homologues of naphthalene.
In testimony whereof I have hereunto set my hand.
IAN C. SOMERVILLE.
acid (66 B.) are heated together for two hoursat 160 C. with constant stirring. The
mass is then cooled to 120 C. and a mixture of 128 grams isopropyl alcohol, 88 grams sulfuric acid (66 B.) is slowly run in over a period of 1% to 2 hours while the temperature is held at 120 C. with constant stirring-- A further period of 3 hours at 120 C. constant stirring completes the alkylation of the naphthalene sulphonic acid, where upon the mass is cooled and a solution of 20 grams sulfuric acid in 180 grams of water is added.
US268376A 1928-04-07 1928-04-07 Condensed aromatic sulphonic acids and process of making same Expired - Lifetime US1770635A (en)

Priority Applications (1)

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US268376A US1770635A (en) 1928-04-07 1928-04-07 Condensed aromatic sulphonic acids and process of making same

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US268376A US1770635A (en) 1928-04-07 1928-04-07 Condensed aromatic sulphonic acids and process of making same

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